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IUBMB Comments Requires Mg2+ . Isolated from Pinus contorta (lodgepole pine) as cyclase I and from Conocephalum conicum (liverwort) .
The enzyme appears in viruses and cellular organisms
Synonyms (-)-sabinene synthase, more
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geranyl diphosphate = (-)-sabinene + diphosphate
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geranyl-diphosphate diphosphate-lyase [cyclizing, (-)-sabinene-forming]
Requires Mg2+. Isolated from Pinus contorta (lodgepole pine) as cyclase I [1] and from Conocephalum conicum (liverwort) [2].
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geranyl diphosphate
(-)-sabinene + diphosphate
geranyl diphosphate + H2O
(-)-sabinene + diphosphate
Substrates: - Products: 52% 1,8-cineole plus 0.6% (+)-alpha-thujene, 1.9% (2)-(1S)-alpha-pinene, 14.5% (-)-sabinene, 7.8% (2)-(1S)-beta-pinene, 13.3% myrcene, 4.0% (2)-(4S)-limonene, (E)-2.7% beta-ocimene, 0.8% terpinolene, and 2.4% alpha-terpineol
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additional information
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geranyl diphosphate
(-)-sabinene + diphosphate
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Substrates: - Products: sole products
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geranyl diphosphate
(-)-sabinene + diphosphate
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Substrates: - Products: wild-type produces 1.3% (+)-car-3-ene, 44.7% (-)-sabinene, 35.9% terpinolene
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geranyl diphosphate
(-)-sabinene + diphosphate
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Substrates: - Products: products are 51.4% (-)-sabinene, 45.8% terpinolene, 2.8% alpha-pinene
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additional information
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Substrates: no substrate: farnesyl diphosphate Products: -
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additional information
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Substrates: no substrate: farnesyl diphosphate Products: -
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Cs+
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or Rb+, K+, NH4+, required
K+
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or Rb+, Cs+, NH4+, required
NH4+
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or Rb+, Cs+, K+, required
Rb+
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or K+, Cs+, NH4+, required
Fe2+
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90% of the activity with Mg2+
Mg2+
or Mn2+, absolutely required. Fully active at 40 mM
Mg2+
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divalent cation absolutely required, with Mg2+ preferred
Mn2+
or Mg2+, absolutely required. Fully active at 1 mM
additional information
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divalent cation absolutely required, with Mg2+ preferred. Activity with cations in decreasing order: Mg2+ > Fe2+ >Mn2+> Zn2+>Co2+ > Ni2+ >Cu2+
additional information
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divalent cation absolutely required, Mg2+ is ineffective. Monovalent cation absolutely required, Li+ and Na+ are ineffective
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0.0002 - 0.0357
geranyl diphosphate
0.0002
geranyl diphosphate
temperature not specified in the publication, pH not specified in the publication
0.004
geranyl diphosphate
-
pH 7.0, 32Ā°C
0.0202
geranyl diphosphate
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mutant A595G/F596L/L599F, 30Ā°C, pH not specified in the publication
0.0316
geranyl diphosphate
-
mutant F596L, 30Ā°C, pH not specified in the publication
0.0357
geranyl diphosphate
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wild-type, 30Ā°C, pH not specified in the publication
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0.001 - 0.545
geranyl diphosphate
0.001
geranyl diphosphate
temperature not specified in the publication, pH not specified in the publication
0.0352
geranyl diphosphate
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mutant A595G/F596L/L599F, 30Ā°C, pH not specified in the publication
0.0825
geranyl diphosphate
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mutant F596L, 30Ā°C, pH not specified in the publication
0.545
geranyl diphosphate
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wild-type, 30Ā°C, pH not specified in the publication
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0.0017 - 0.0153
geranyl diphosphate
0.0017
geranyl diphosphate
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mutant A595G/F596L/L599F, 30Ā°C, pH not specified in the publication
0.0027
geranyl diphosphate
-
mutant F596L, 30Ā°C, pH not specified in the publication
0.0153
geranyl diphosphate
-
wild-type, 30Ā°C, pH not specified in the publication
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6.6
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half-maximal activity
7.8
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80% of maximum activity
8
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80% of maximum activity
8.5
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half-maximal activity
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brenda
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UniProt
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isoform 2
UniProt
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promoter activity is primarily found in the epidermis, cortex, and stele of mature primary and lateral roots, but not in the root meristem or the elongation zone
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promoter activity is primarily found in the epidermis, cortex, and stele of mature primary and lateral roots, but not in the root meristem or the elongation zone
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promoter activity is primarily found in the epidermis, cortex, and stele of mature primary and lateral roots, but not in the root meristem or the elongation zone
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Highest Expressing Human Cell Lines
Filter by:
Cell Line Links
Gene Links
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ATERP_PINCO
616
0
70590
Swiss-Prot
Chloroplast (Reliability: 2 )
CIN1_ARATH
600
0
70455
Swiss-Prot
-
CIN2_ARATH
600
0
70455
Swiss-Prot
-
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60000
x * 60000, SDS-PAGE
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A595G
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shift in product profile, mutant produces 2.4% (+)-car-3-ene, 39% (-)-sabinene, 33.3% terpinolene
A595G/F596L/L599F
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shift in product profile, mutant produces 42.3% (+)-car-3-ene, 7.3% (-)-sabinene, 20.1% terpinolene
F596E
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shift in product profile, mutant produces 0.5% (+)-car-3-ene, 10.2% (-)-sabinene, 5.7% terpinolene, 70.9% limonene
F596G
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shift in product profile, mutant produces 10.0% (+)-car-3-ene, 11.2% (-)-sabinene, 17.3% terpinolene, 27.0% myrcene, 17.0% limonene
F596H
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shift in product profile, mutant produces 2.1% (+)-car-3-ene, 46.5% (-)-sabinene, 27.1% terpinolene
F596L
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shift in product profile, mutant produces 28.6% (+)-car-3-ene, 42.8% (-)-sabinene, 36.4% terpinolene
L599F
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shift in product profile, mutant produces 1.5% (+)-car-3-ene, 20.2% (-)-sabinene, 32.2% terpinolene
S589A
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shift in product profile, mutant produces 1.2% (+)-car-3-ene, 42.9% (-)-sabinene, 35.5% terpinolene
additional information
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construction of a series of domain swaps and site-directed substitutions between (-)-sabinene synthase and (+)-3-carene synthase isoforms to explore which regions and specific amino acids of these enzymes affect the differences of their product profiles. The amino acid in position 596 is critical for product profiles dominated by or (-)-sabinene. A leucine in this position promotes formation of (+)-3-carene, whereas phenylalanine promotes (-)-sabinene
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7
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most stable at pH 7.0
3777
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expression in Escherichia coli
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Adam, K.P.; Croteau, R.
Monoterpene biosynthesis in the liverwort Conocephalum conicum: demonstration of sabinene synthase and bornyl diphosphate synthase
Phytochemistry
49
475-480
1998
Conocephalum conicum
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Savage, T.J.; Ichii, H.; Hume, S.D.; Little, D.B.; Croteau, R.
Monoterpene synthases from Gymnosperms and Angiosperms: stereospecificity and inactivation by cysteinyl- and arginyl-directed modifying reagents
Arch. Biochem. Biophys.
269
4012-4020
1994
Pinus contorta
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Chen, F.; Ro, D.K.; Petri, J.; Gershenzon, J.; Bohlmann, J.; Pichersky, E.; Tholl, D.
Characterization of a root-specific Arabidopsis terpene synthase responsible for the formation of the volatile monoterpene 1,8-cineole
Plant Physiol.
135
1956-1966
2004
Arabidopsis thaliana (P0DI76), Arabidopsis thaliana (P0DI77)
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Roach, C.R.; Hall, D.E.; Zerbe, P.; Bohlmann, J.
Plasticity and evolution of (+)-3-carene synthase and (-)-sabinene synthase functions of a Sitka spruce monoterpene synthase gene family associated with weevil resistance
J. Biol. Chem.
289
23859-23869
2014
Picea sitchensis
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